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RPL30P10 ribosomal protein L30 pseudogene 10 [ Homo sapiens (human) ]

Gene ID: 100270982, updated on 10-Oct-2023

Summary

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Official Symbol
RPL30P10provided by HGNC
Official Full Name
ribosomal protein L30 pseudogene 10provided by HGNC
Primary source
HGNC:HGNC:36822
See related
Ensembl:ENSG00000243050 AllianceGenome:HGNC:36822
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
RPL30_5_906
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Genomic context

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Location:
8q12.1
Annotation release Status Assembly Chr Location
RS_2023_10 current GRCh38.p14 (GCF_000001405.40) 8 NC_000008.11 (57392546..57392882)
RS_2023_10 current T2T-CHM13v2.0 (GCF_009914755.1) 8 NC_060932.1 (57814085..57814421)
105.20220307 previous assembly GRCh37.p13 (GCF_000001405.25) 8 NC_000008.10 (58305105..58305441)

Chromosome 8 - NC_000008.11Genomic Context describing neighboring genes Neighboring gene RNA, U6 small nuclear 596, pseudogene Neighboring gene Sharpr-MPRA regulatory region 3559 Neighboring gene uncharacterized LOC101929488 Neighboring gene uncharacterized LOC107986888 Neighboring gene NANOG hESC enhancer GRCh37_chr8:58355141-58355642 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr8:58368641-58369219 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 27404 Neighboring gene uncharacterized LOC105375855 Neighboring gene NANOG hESC enhancer GRCh37_chr8:58381292-58381935

Genomic regions, transcripts, and products

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Go to nucleotide: Graphics FASTA GenBank

Bibliography

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Related articles in PubMed

  1. Comparative analysis of processed ribosomal protein pseudogenes in four mammalian genomes. Balasubramanian S, et al. Genome Biol, 2009. PMID 19123937, Free PMC Article

GeneRIFs: Gene References Into Functions

Phenotypes

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Review eQTL and phenotype association data in this region using PheGenI

Variation

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See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

General gene information

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NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

Genomic

  1. NG_010695.1 

    Range
    101..437
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2023_10

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000008.11 Reference GRCh38.p14 Primary Assembly

    Range
    57392546..57392882
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060932.1 Alternate T2T-CHM13v2.0

    Range
    57814085..57814421
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)
Nucleotide Protein
Heading Accession and Version

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